The Seckel syndrome: A case observed in the pediatric department of the University Hospital Center Sourou Sanou (Burkina Faso)

Seckel syndrome-1 or “bird-headed dwarfism”, Online Mendelian Inheritance in Man number 210600, is a rare genetic disease with an autosomal recessive transmission. We report a female child of 56 months diagnosed with SCKL1 at the Pediatric department of the University Hospital Center Sourou Sanou, B...

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Dettagli Bibliografici
Pubblicato in:Pediatr Rep
Autori principali: Ouattara, Ad Bafa Ibrahim, Barro, Makoura, Nacro, Sahoura Fatimata, Traoré, Ibraïma, Sanogo, Bintou, Diallo, Jean W., Nacro, Boubacar
Natura: Artigo
Lingua:Inglês
Pubblicazione: PAGEPress Scientific Publications, Pavia, Italy 2020
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7160856/
https://ncbi.nlm.nih.gov/pubmed/32308969
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/pr.2020.8231
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